HPV Virology and Treatment

Introduction

HPV currently infects twenty million Americans and about another six million become infected each year. Today, at least fifty percent of sexually active men and women get HPV during their lifetime (40). As one can see, this sexually transmitted disease is among the most prevalent in America, which explains the importance of understand the disease. Human papillomavirus (HPV) or the “wart virus” is a virus belonging to its own family, papillomaviridae. There are more than a 100 types of HPV and as reflected in its name, species specific for humans. There are two types, cutaneous or mucocutaneous, based upon its tissue tropism or predilection for infecting specific areas of the human body. Human papillomavirus infections are diagnosed worldwide, account for the most common sexually transmitted disease worldwide, and have been associated with both cutaneous and mucocutaneous cancers prompting attempts to prevent infections using vaccines. In short, it has become a global health infection warranting every effort to control and eradicate it.

The Virology of HPV

Virology/Oncogenesis/Molecular detection

HPV is a double-stranded DNA, non-enveloped capsid virus. It has 7900 base pairs which have 90% homology between the types (1). The base pairs are arranged in a circle which includes the codes for two key proteins known as L1 and L2 (2). These two proteins act as the “immunogene” which is required for self-assembly and the infectivity protein, respectively (2,3). The virus is transmitted between humans through breaks within the epidermis of the skin. Once the virus enters the skin, it attaches to a component of skin stem cells known as the tissue-specific heparin sulfate proteoglycans (4,5,6). Differentiation of the virus then occurs within the squamous keratinocyte (7), replicates, proliferates, and then moves to the next cell. It is the persistence of HPV within the squamous which poses the greatest risk for malignant degeneration. [See the figure from Robert W. Trindle, Nature Reviews Cancer 2:59-64, 2002]

HPV types are differentiated by their associations with specific types of human cancers. For example, HPV 16 and 18 are most frequently associated with cervical cancer (8). HPV 16 accounts for up to 50% of HPV causing cervical and anal cancers worldwide (8,9,10). In addition of those viruses associated with penile cancer, 70% are of the HPV 16 phenotype and occurs 6 times higher in males with histories of venereal warts or condylomata accuminata.

HPVs have been proven to be the causative agents of other epithelial cancers. The proof that these viruses indeed are the causative agents is based upon the following observations (11):

1)HPV DNA has been found within cancer biopsies 2)known viral oncogenes E6 and E7 are found in cancer material 3)genes E6 and E7 code for proteins which are growth-regulators in host cells 4)E6 and E7 gene expression have been identified in cervical cancer immortalized cell lines(12) 5)epidemiologic investigations have identified HPV as a major factor for the development of cervical cancer 6)species specific papillomaviruses cause cancer in experimental animal models including the rabbit and cow; and human neonatal foreskin infected with HPV-16 and placed in severe combined immunodeficient mice form intraepithelial neoplasms (Mandel)

Molecular pathogenesis of skin cancer implicates HPV-E6 gene product binding to the human p53 tumor suppressor protein as the initial event (13-16). The p53 protein is a negative regulator the cell cycle transformation step between G0/G1 to the S phase. By degrading the p53 protein cell growth is directly impeded. E7 appears to exert an anti-cell death (anti-apoptotic) effect in cells through mutations in the p53 protein (17, 18) by interfering with the G1 or arrest phase of the cell cycle. Thus, both genes negatively impact normal cell cycles causing an unregulated, unimpeded cell growth, i.e. cancer transformation.

HPV is now generally detected in human tissue by various molecular biologic techniques including in situ hybridization (ISH), Southern transfer hybridization (STH), hybrid capture (HC), dot blot (DB), filter hybridization (FH), or polymerase chain reaction (PCR) (19). ISH is sensitive and can be performed directly on infected tissue specimens. It is both tedious and less sensitive than PCR and HC and thus rarely used. DB, FH, and STH are reserved for research studies and are capable of providing separations among the HPV types. HC requires a long single-stranded RNA probe to hybridize with a whole HPV genome in solution. This test enables identification of specific HPVs and quantifies them. It currently is the only method approved by the Federal Drug Administration in the United States for detection of HPV in cervical samples. PCR remains the most sensitive method for detection. It utilizes a specific primer sequence for a specific type of HPV which as a result can be used to verify links between the virus and various types of human cancers.

The Epidemiology of HPV

Epidemiology

HPV is both ubiquitous and ever prevalent in humans worldwide. A worldwide investigation of over 150,000 women with normal Pap smears (cervical cytology) revealed HPV prevalence at approximately 10% (20). Of all the regions of the world, African remains the continent with the highest prevalence of HPV infections (22% of the women examined) and incidence of the carcinogenic HPV types, 16 and 18. [See the figure from Lancet Infect Dis. de Sanjose et al. 207(7):453-459, 2007]

Prevalence of cervical HPV infections peaks by age 30 years then drops quickly. This corresponds to the greatest periods of sexual activity among women (21). Of interest is the finding women in Europe are more likely to become infected with HPV 16 than those in Sub-Saharan Africa (22). In certain African countries such as Uganda, HPV prevalence can exceed 75% although the major types were equally distributed between 16, 18, 51 and 52. In the United States 75-80% of sexually active adults acquire anon-genital infections by the age of 50 years (23). The highest prevalence group (45%) was women between the ages of 20 and 24 years. A study of approximately 250 female college students found as many as 29% developed an HPV infection after their first sexual encounter (24). It is important to note that most infections are transient. One study of 431 women, half of whom had anal HPV, found that 60% had cleared their infections within 15 months after detection (25). Chronic infections are more likely associated with those of the cervix and may account for the greater incidence of cervical cancer versus anal cancer due to HPV.

Males are also at risk for HPV infections with prevalence rates between 1-70% (26). Risk factors include sexual behavior (men having sex with men vs. heterosexual men), circumcision, condom use, prior STDs (sexually transmitted diseases), race and ethnicity (27,28). Among HIV negative homosexual men the prevalence rate is approximately 50% whereas in heterosexual males, cigarette smokes and those who had intercourse with multiple female partners were associated with higher rates. Condom use was associated with the lowest prevalent rates. Again, in males like females infections were cleared within 12 months in as many as 75% of those originally infected (29). Circumcision confers an advantage for clearing the infection by almost 6-fold within 12 months versus in non-circumcised males (30).

Human Diseases of HPV

Although most epidemiologic studies of HPV infections involve STD studies, HPV infections are not limited to mucocutaneous areas. Warts of the epidermis occur in approximately 10% of all children with peak ages between 12 to 16 years (31). It is estimated that 4% of adults have non-genital warts at any given time (32). These warts can be associated with skin cancer but only rarely. Prevalence of genital warts in the United States is estimated at 1% while as high as 10% in the Scandinavian countries (31, 33, 34). Unfortunately in some studies the oncogenic strains HPV 16 and 18, can account 50% and 15% of the cases worldwide (8). More than 350,000 cases of cervical cancer are diagnosed annually (35). These same HPV types have been implicated in cancers of the head and neck. The table below lists the various HPV diseases that can affect humans. (Refer to Table. Adapted from Mandell, Douglas, and Bennett’s Principles and Practice of Infectious Disease. 7th Ed. 2009. Churchill Livingstone, Philadelphia. V.2. Chapter 144: Papillomaviruses. Section Eds. William Bounez and Richard C. Reichman).

Respiratory papillomatosis is an unusual form of HPV disease. It presents in children between the ages of 6 and 10 years, all having been delivered as vaginal births, with signs of respiratory tract obstruction. The obstruction usually is at the larynx (voice box). Lesions can be recurrent and are difficult to treat. (36).

The Treatment and Prevention of HPV

Treatment

Treatment of HPV infections usually is aimed at ablation or eradication. However, cutaneous warts resolve without treatment 60% of the time within 3 to 24 months (31,37). Anogenital warts require aggressive treatments (ablative or immune modulation) but are successful only 75% of the time with recurrence rates at 25% (38).

Treatments can consist of surgical removal, immune modulation or physical/chemical destruction. The latter form is the basis of most over the counter remedies which can be purchased at your local pharmacy. Podophyllin is the major ingredient in this form and is applied directly to the wart. Immune modulation by the drug imiquimod, causes alpha and gamma interferon and interleukins to be produced locally aiding in T-cell cytoxic reactions. More potent treatments are administered by licensed practitioners and include trichloroacetic acid, 5-fluorouracil, or alpha interferon injections. Surgical options include cryotherapy, laser therapy, electrocautery, and excision (Mandel). Options for therapy ought to be directed toward a trained clinician.

Prevention

Prevention is currently the most successful means of controlling HPV genital infections. As stated above condom use clearly prevents transmission of the disease and lowers the risk of recurrence substantially. However, the most far-reaching means to control HPV associated cervical cancer was the introduction of the vaccine, Gardasil (Merck, West Point, PA; Mandel) in 2006. This is a quadrivalent vaccine directed against types 6, 11, 16, and 18. This vaccine is given three times at month 0, 2 and 6. A second vaccine is under production for only the type 16 and 18 HPVs. Its efficaciousness is considered remarkable and in the range of 80-90% (Mandel). This vaccine has not only shown protection from the infection by the four types of HPVs but has prevented future warts and intraepithelial cancers in females. For males it has not demonstrated prevention of penile cancer (Mandel). Despite this success the vaccine has not met with worldwide approval (39). Current efforts for vaccine trials include vaccinating both male and female sexual partners. The following figure helps to explain the benefits of immune modulation via vaccines despite the reluctance to universally vaccinate individuals prior to their becoming sexually active adults (Einstein ME et al. Lancet Infect Dis 9:347-356, 2009; Figure p.349).

Conclusion

Overall paper length should be approximately 2,000 to 2,500 words.
Include at least two data figures.
Use professional sources, including at least two research studies. Public Health Measures Against HPV

References

General reviews:

Mandell, Douglas, and Bennett’s Principles and Practice of Infectious Disease. 7th Ed. 2009. Churchill Livingstone, Philadelphia. V.2. Chapter 144: Papillomaviruses. Section Eds. William Bounez and Richard C. Reichman.

Wheeler, CM. Natural history of human papillomavirus infections, cytologic and histologic abnormalities, and cancer. Obstr Gynecol Clin. 35 (4) Dec 2008; pp.519-536.

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